| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 152951 | BAA02g01450 | A02 | 664485 | C | T | synonymous_variant | LOW | c.288C>T|p.Ser96Ser |
S1 S90 |
| 152952 | BAA02g01460 | A02 | 665108 | G | A | missense_variant | MODERATE | c.382C>T|p.Arg128Trp |
S232 |
| 152953 | BAA02g01460 | A02 | 666295 | G | A | upstream_gene_variant | MODIFIER | c.-806C>T| |
S162 |
| 152954 | BAA02g01460 | A02 | 666692 | G | A | upstream_gene_variant | MODIFIER | c.-1203C>T| |
S84 |
| 152955 | BAA02g01460 | A02 | 666929 | G | A | upstream_gene_variant | MODIFIER | c.-1440C>T| |
S41 |
| 152956 | BAA02g01460 | A02 | 668651 | G | A | upstream_gene_variant | MODIFIER | c.-3162C>T| |
S153 S213 |
| 152957 | BAA02g01470 | A02 | 674014 | G | A | synonymous_variant | LOW | c.1107G>A|p.Gly369Gly |
S183 S198 |
| 152958 | BAA02g01470 | A02 | 674070 | G | A | missense_variant | MODERATE | c.1163G>A|p.Arg388Lys |
S125 |
| 152959 | BAA02g01470 | A02 | 674776 | G | A | synonymous_variant | LOW | c.1869G>A|p.Glu623Glu |
S208 S93 |
| 152960 | BAA02g01470 | A02 | 674924 | G | A | missense_variant | MODERATE | c.2017G>A|p.Gly673Ser |
S161 |
| 152961 | BAA02g01470 | A02 | 675366 | A | T | downstream_gene_variant | MODIFIER | c.*305A>T| |
S174 |
| 152962 | BAA02g01480 | A02 | 676925 | G | A | missense_variant | MODERATE | c.1232C>T|p.Ser411Phe |
S43 |
| 152963 | BAA02g01480 | A02 | 677409 | G | A | missense_variant | MODERATE | c.748C>T|p.His250Tyr |
S297 |
| 152964 | BAA02g01480 | A02 | 678305 | C | T | upstream_gene_variant | MODIFIER | c.-149G>A| |
S211 S227 |
| 152965 | BAA02g01480 | A02 | 679431 | G | A | upstream_gene_variant | MODIFIER | c.-1275C>T| |
S260 |
| 152966 | BAA02g01480 | A02 | 679557 | C | T | upstream_gene_variant | MODIFIER | c.-1401G>A| |
S19 |
| 152967 | BAA02g01480 | A02 | 679651 | G | A | upstream_gene_variant | MODIFIER | c.-1495C>T| |
S134 |
| 152968 | BAA02g01490 | A02 | 680289 | G | A | missense_variant | MODERATE | c.2456C>T|p.Ser819Phe |
S289 S290 |
| 152969 | BAA02g01490 | A02 | 680358 | C | T | missense_variant | MODERATE | c.2387G>A|p.Gly796Asp |
S246 |
| 152970 | BAA02g01490 | A02 | 680386 | C | T | missense_variant | MODERATE | c.2359G>A|p.Glu787Lys |
S194 |
| 152971 | BAA02g01490 | A02 | 680561 | C | T | synonymous_variant | LOW | c.2184G>A|p.Val728Val |
S6 |
| 152972 | BAA02g01490 | A02 | 680598 | C | T | missense_variant | MODERATE | c.2147G>A|p.Arg716Lys |
S280 |
| 152973 | BAA02g01490 | A02 | 680704 | C | T | missense_variant | MODERATE | c.2041G>A|p.Glu681Lys |
S2 |
| 152974 | BAA02g01490 | A02 | 681055 | C | T | synonymous_variant | LOW | c.1761G>A|p.Glu587Glu |
S167 |
| 152975 | BAA02g01490 | A02 | 681644 | C | T | missense_variant | MODERATE | c.1495G>A|p.Glu499Lys |
S120 |